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Literature DB >> 7573165

Cutaneous manifestations of Apert syndrome.

M M Cohen, S Kreiborg.

Abstract

Entities: Disease

Mesh：

Year: 1995 PMID： 7573165 DOI： 10.1002/ajmg.1320580119

Source DB: PubMed Journal: Am J Med Genet ISSN： 0148-7299

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8 in total

Review 1. The molecular and cellular basis of Apert syndrome.

Authors: Chao Liu; Yazhou Cui; Jing Luan; Xiaoyan Zhou; Jinxiang Han
Journal: Intractable Rare Dis Res Date: 2013-11

2. Role of FGFR2-signaling in the pathogenesis of acne.

Authors: Bodo C Melnik
Journal: Dermatoendocrinol Date: 2009-05

3. Cranio-maxillofacial, orthodontic and dental treatment in three patients with Apert syndrome.

Authors: S Carpentier; J Schoenaers; C Carels; A Verdonck
Journal: Eur Arch Paediatr Dent Date: 2014-03-19

Review 4. Craniosynostosis as a clinical and diagnostic problem: molecular pathology and genetic counseling.

Authors: Anna Kutkowska-Kaźmierczak; Monika Gos; Ewa Obersztyn
Journal: J Appl Genet Date: 2018-02-01 Impact factor: 3.240

5. Biochemical analysis of pathogenic ligand-dependent FGFR2 mutations suggests distinct pathophysiological mechanisms for craniofacial and limb abnormalities.

Authors: Omar A Ibrahimi; Fuming Zhang; Anna V Eliseenkova; Nobuyuki Itoh; Robert J Linhardt; Moosa Mohammadi
Journal: Hum Mol Genet Date: 2004-07-28 Impact factor: 6.150

Cutaneous manifestations of Apert syndrome.

Review 1. The molecular and cellular basis of Apert syndrome.

2. Role of FGFR2-signaling in the pathogenesis of acne.

3. Cranio-maxillofacial, orthodontic and dental treatment in three patients with Apert syndrome.

Review 4. Craniosynostosis as a clinical and diagnostic problem: molecular pathology and genetic counseling.

5. Biochemical analysis of pathogenic ligand-dependent FGFR2 mutations suggests distinct pathophysiological mechanisms for craniofacial and limb abnormalities.

Review 6. Syndromic Craniosynostosis: Complexities of Clinical Care.

7. [Apert syndrome in a 60-year old Congolese: about one observation].

8. Clinical study and some molecular features of Mexican patients with syndromic craniosynostosis.